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2-Azabicyclo[2.2.1]heptane-2-carboxylic acid, 5-hydroxy-, phenylMethyl ester is a heterocyclic phenylmethyl ester derivative characterized by a seven-membered ring with a nitrogen atom and a carboxylic acid group. 2-Azabicyclo[2.2.1]heptane-2-carboxylic acid, 5-hydroxy-, phenylMethyl ester features a phenylmethyl ester functional group, which is commonly used to protect sensitive functional groups in organic chemistry. Its potential applications in pharmaceuticals and as a chemical intermediate in organic synthesis are subject to further research and analysis.

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  • 1217190-38-9 Structure
  • Basic information

    1. Product Name: 2-Azabicyclo[2.2.1]heptane-2-carboxylic acid, 5-hydroxy-, phenylMethyl ester
    2. Synonyms: 2-Azabicyclo[2.2.1]heptane-2-carboxylic acid, 5-hydroxy-, phenylMethyl ester;(1R,4R,5S)-benzyl 5-hydroxy-2-azabicyclo[2.2.1]heptane-2-carboxylate
    3. CAS NO:1217190-38-9
    4. Molecular Formula: C14H17NO3
    5. Molecular Weight: 247.28968
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1217190-38-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-Azabicyclo[2.2.1]heptane-2-carboxylic acid, 5-hydroxy-, phenylMethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Azabicyclo[2.2.1]heptane-2-carboxylic acid, 5-hydroxy-, phenylMethyl ester(1217190-38-9)
    11. EPA Substance Registry System: 2-Azabicyclo[2.2.1]heptane-2-carboxylic acid, 5-hydroxy-, phenylMethyl ester(1217190-38-9)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1217190-38-9(Hazardous Substances Data)

1217190-38-9 Usage

Uses

Used in Pharmaceutical Industry:
2-Azabicyclo[2.2.1]heptane-2-carboxylic acid, 5-hydroxy-, phenylMethyl ester is used as a pharmaceutical candidate for its potential therapeutic properties. The heterocyclic structure and phenylmethyl ester group may contribute to its interaction with biological targets, offering potential benefits in drug development.
Used in Organic Synthesis:
In the field of organic synthesis, 2-Azabicyclo[2.2.1]heptane-2-carboxylic acid, 5-hydroxy-, phenylMethyl ester serves as a chemical intermediate. Its unique structure and functional groups can be utilized in the synthesis of more complex molecules, contributing to the advancement of chemical research and the development of new compounds with various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1217190-38-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,1,7,1,9 and 0 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1217190-38:
(9*1)+(8*2)+(7*1)+(6*7)+(5*1)+(4*9)+(3*0)+(2*3)+(1*8)=129
129 % 10 = 9
So 1217190-38-9 is a valid CAS Registry Number.

1217190-38-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzyl 5-hydroxy-2-azabicyclo[2.2.1]heptane-2-carboxylate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1217190-38-9 SDS

1217190-38-9Relevant articles and documents

IMIDAZOLE DERIVATIVES

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Page/Page column 98-99, (2013/02/27)

Described herein are compounds of formula (I), The compounds of formula I act as DGAT1 inhibitors and can be useful in preventing, treating or acting as a remedial agent for hyperlipidemia, diabetes mellitus and obesity.

Histamine H3 Inverse Agonists and Antagonists and Methods of Use Thereof

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Page/Page column 65-66, (2011/04/18)

Provided herein are fused imidazolyl compounds, methods of synthesis, and methods of use thereof. The compounds provided herein are useful for the treatment, prevention, and/or management of various disorders, including, e.g., neurological disorders and metabolic disorders. Compounds provided herein inhibit the activity of histamine H3 receptors and modulate the release of various neurotransmitters, such as, e.g., histamine, acetylcholine, norepinephrine, and dopamine (e.g. at the synapse). Pharmaceutical compositions containing the compounds and their methods of use are also provided herein.

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